Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4647608
rs4647608
1 4 184647083 intron variant C/T snv 1.7E-04 0.700 1.000 1 2012 2012
dbSNP: rs4647614
rs4647614
1 4 184646349 intron variant T/C snv 5.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs4647665
rs4647665
1 4 184634712 intron variant A/G snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs4647667
rs4647667
1 4 184634471 intron variant G/A snv 1.7E-02 0.700 1.000 1 2012 2012